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Volumn 84, Issue 8, 2012, Pages 1673-1684

Accessing chemical diversity by stereoselective gold-catalyzed manipulation of allylic and propargylic alcohols

Author keywords

Asymmetric catalysis; Gold; Heterocyclic chemistry

Indexed keywords

ALKYLATING AGENTS; ALLYLIC ALCOHOL; ASYMMETRIC CATALYSIS; AU-COMPLEXES; BOND FORMING; CHEMICAL DIVERSITY; DIRECT ACTIVATION; MORPHOLINES; PROPARGYLIC ALCOHOLS; STEREO-SELECTIVE; STEREOSELECTIVE MANNER;

EID: 84864451657     PISSN: 00334545     EISSN: 13653075     Source Type: Journal    
DOI: 10.1351/PAC-CON-11-09-05     Document Type: Article
Times cited : (25)

References (66)
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  • 65
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    • The 6-endo-dig mechanism seems not structurally accessible for compounds 6-type, owing to the limited length of the side chain
    • The 6-endo-dig mechanism seems not structurally accessible for compounds 6-type, owing to the limited length of the side chain.
  • 66
    • 84864428464 scopus 로고    scopus 로고
    • Analogous regiochemical response was reported in literature in the Au-catalyzed hydroindolination of unfunctionalized internal alkynes (see ref. [23])
    • Analogous regiochemical response was reported in literature in the Au-catalyzed hydroindolination of unfunctionalized internal alkynes (see ref. [23]).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.